Clinical Research Coordinator I - Start in Clinical Trials

Mount Sinai

New York (NY)

On-site

USD 59,000 - 74,000

Full time

4 days ago
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Job summary

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily clinical study activities, obtain informed consent, and maintain study data. You will assist with grant applications and regulatory submissions, and manage source documents and subject files in alignment with hospital procedures.

Role involves coordinating with investigators, monitoring visits, and ensuring accurate data collection and timely communications with sponsoring agencies.

Qualifications

  • Bachelor's or Master's degree in Science or closely related field.
  • No experience required; one year of research experience preferred.

Responsibilities

  • Collects and records study data. Inputs all information into database.
  • Obtains informed consent under minimal supervision and educates participants regarding study requirements.
  • Assists in the activities related to clinical research studies including screening participants for eligibility and registering subjects with sponsoring agency.
  • Assists in preparing grant applications, IRB/GCO for submission and filings.
  • Maintains source documents and subject files in accordance with hospital procedures; ensures complete compilation of subject data through chart reviews.
  • Secures, delivers and ships clinical specimens as required by the protocol.
  • Prepares for monitoring visits.
  • Performs other related duties.

Education

Bachelors or Masters degree in Science or closely related field

Job description

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to support daily clinical study activities, obtain informed consent, and maintain study data. You will assist with grant applications and regulatory submissions, and manage source documents and subject files in alignment with hospital procedures.

Role involves coordinating with investigators, monitoring visits, and ensuring accurate data collection and timely communications with sponsoring agencies.

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